International safety notice
Corrective action for the Ascenda™ Intrathecal Catheters / Revision Kits, Medtronic
Germany / BfArM · DEU · Jul 22, 2014
Key facts
| Title | Corrective action for the Ascenda™ Intrathecal Catheters / Revision Kits, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Ascenda™ Intrathecal Catheters / Revision Kits, Medtronic |
| Manufacturer | Corrective action for the Ascenda™ Intrathecal Catheters / Revision Kits, Medtronic |
| Models | 0208453608, 0208408598, 0208453197, 0208453907, 0208448422, 0208438524, 0208422783, 0208477579, 0208461924, 0208422620, 0208439147, 0208408595 and 233 more |
| Date | Jul 22, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1